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An interventional non-randomized controlled study of Mongolian Mind–Body Interactive therapy on essential hypertension

An interventional non-randomized controlled study of Mongolian Mind–Body Interactive therapy on essential hypertension

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087816
Enrollment
Unknown
Registered
2024-08-05
Start date
2024-06-19
Completion date
Unknown
Last updated
2024-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

essential hypertension

Interventions

control group:Oral administration of dipine antihypertensive drugs and Mongolian Mind–Body Interactive therapy
experimental group:Mongolian Mind–Body Interactive therapy

Sponsors

Inner Mongolia Traditional Chinese& Mongolian Medical Research Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Age range from 45 to 60 years old, regardless of gender; ? Primary hypertension (diagnosed based on the revised 2018 edition of the Chinese Guidelines for the Prevention and Treatment of Hypertension) is a mild to moderate condition that meets the diagnostic criteria for primary hypertension and meets the risk classification for hypertension: low or medium risk. Patients who have not taken antihypertensive drugs since diagnosis or have only taken dipine antihypertensive drugs; ? Be able to maintain contact and cooperate with the requirements of this study during the treatment period; ? If the four tests for infection are negative, an electrocardiogram and liver, gallbladder, pancreas, spleen, kidney, and portal vein system examination in the past week can be provided; ? Can provide clinical examination project reports for the past half month: EEG, 24-hour dynamic electrocardiogram, chest CT, abdominal ultrasound (liver, gallbladder, pancreas, spleen, kidney, and portal vein system examination), cardiac color Doppler ultrasound examination, blood routine, major biochemistry (liver function, kidney function, ions, blood glucose, blood lipids, myocardial enzyme spectrum, etc.), inflammatory factors (C-reactive protein (CPR) measurement, erythrocyte sedimentation rate (ESR) measurement); ? Collaborate with collecting peripheral blood four times (before treatment and after 1, 4, and 8 weeks of treatment), as well as morning urine and saliva. ? Those who voluntarily participate in this clinical study and sign informed consent.

Exclusion criteria

Exclusion criteria: ? Pregnant, breastfeeding, or taking birth control pills. ? Patients who are currently participating in other clinical trials or have participated in other clinical trials within the past month. ? Patients who have consumed Western medicine, Mongolian medicine, traditional Chinese medicine, or other traditional medicine treatments other than antihypertensive drugs within 2 weeks, as well as those who have participated in Mongolian medicine psychosomatic interaction therapy, need to stop for more than 2 weeks before they can participate in this study. ? Having a current state or medical history of mental illness, or a history of alcohol or drug abuse, which affects compliance with the research protocol. ? And any other circumstances that may affect the research results, as determined by the doctor.

Design outcomes

Primary

MeasureTime frame
blood pressure;SF36;

Secondary

MeasureTime frame
electroencephalogram;C-reactive protein;Self Rating Depression Scale;Anxiety Self Rating Scale;

Countries

China

Contacts

Public ContactNAGONGBILIGE

Inner Mongolia Traditional Chinese& Mongolian Medical Research Institute

340695804@qq.com+86 471 359 9386

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026